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inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing
The detection of copy number variations (CNVs) on whole-exome sequencing (WES) represents a cost-effective technique for the study of genetic variants. This approach, however, has encountered an obstacle with high false-positive rates due to biases from exome sequencing capture kits and GC contents....
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| I publikationen: | Evol Bioinform Online |
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| Huvudupphovsmän: | , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
SAGE Publications
2020
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7520931/ https://ncbi.nlm.nih.gov/pubmed/33029071 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1176934320956577 |
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